电场与MnxCey催化剂在苯氧化反应中的协同效应及机理探究

挥发性有机物（VOCs）大量排放已成为日益严重的环境问题,为了实现VOCs的高效去除,本文采用自蔓延燃烧合成法制备了一系列锰铈复合氧化物催化剂,将稳恒直流电场引入典型VOCs气体苯的催化氧化过程,并基于不同电场条件下催化剂的理化性质表征结果进行机理分析.实验结果表明,Mn_xCe_y催化剂对含苯废气的去除有良好的效果,稳恒直流电场显著促进了催化剂的活性,其中Mn₁Ce₃的催化性能最佳,电流为5 mA时,Mn₁Ce₃催化剂在155℃可达到50%的苯转化率,在202.4℃可达到90%的苯转化率,对应的转化温度T₅₀和T₉₀比传统方法分别降低了62.4℃和48.3℃,且电场中的反应活化能由52.32 kJ·mol^-1降低至32.31 kJ·mol^-1.根据实验现象及表征结果,发现协同效应与活性位点的快速持续再生及活性氧物种的转化有关,由此提出苯在Mn_xCe_y催化剂上的氧化机理及电场协同催化的反应模型.     

外源性稀土La和Ce对几种淡水微藻生长影响的研究

通过模拟培养实验,研究了不同质量浓度的稀土元素La3+和Ce3+对2种产地的微囊藻以及月牙藻增殖的影响.结果表明低质量浓度的La3+和Ce3+对2种微囊藻的刺激作用明显大于对月牙藻的刺激作用,说明稀土元素La3+和Ce3+在湖泊中的富集可能改变湖泊种群结构,有利于微囊藻在湖泊中形成优势种;高质量浓度的La3+和Ce3+对3种藻均有抑制生长的作用,当La3+和Ce3+的质量浓度为50.0 mg/L时,微囊藻的生长繁殖完全被抑制.     

用MnSO4-Ce(SO4)2协同催化快速测定COD的研究

本文探讨了以MnSO4-Ce(SO4)2复合催化剂代替标准重铬酸钾法中的Ag2SO4，用密封消解法测定废水COD值的可行性，研究了复合催化剂总量、配比、消解时间、溶液酸度等因素对COD测定的影响。通过对各种废水COD值的测定表明，用MnSO4-Ce(SO4)2做催化剂，在165℃，较低酸度，密封消解15min是可行的。     

镧、铈对厌氧颗粒污泥产甲烷的Hormesis效应及其动力学研究

间歇培养条件下研究了单一稀土元素镧(La3 )和铈(Ce3 )在不同浓度水平下对厌氧颗粒污泥活性及其动力学行为的影响.结果表明,La3 和Ce3 对厌氧颗粒污泥比产甲烷活性有促进作用的浓度范围均为0.01～0.1 mg·L-1,促进作用浓度峰值均为0.05mg·L-1,最大促进百分比分别为10.35%和20.79%;La3 和Ce3 对SMA(比甲烷活性)的半抑制浓度分别为5mg·L-1和1000mg·L-1,La3 较易对污泥产生抑制作用.米-门方程可以用来描述厌氧消化过程中甲烷发酵阶段的动力学行为,稀土元素La3 和Ce3 投加至反应系统后,提高了甲烷发酵过程的动力学常数Vmax和半饱和常数Ks.     

Effects of cerium on growth and physiological mechanism in plants under enhanced ultraviolet-B radiation

Effect of cerium （Ce^3＋） on the growth, photosynthesis and antioxidant enzyme system in rape seedlings （Brassica juncea L.） exposed to two levels of UV-B radiation （T1： 0.15 W/m^2 and T2：0.35 W/m^2） was studied by hydroponics under laboratory conditions. After 5 d of UV-B treatment, the aboveground growth indices were obviously decreased by 13.2%-44. 1%（T1） and 21.4%-49.3% （T2）, compared to CK, and except active absorption area of roots, the belowground indices by 14.1%-35.6%（T1） and 20.3%-42.6% （T2）. For Ce＋UV-B treatments, the aboveground and belowground growth indices were decreased respectively by 4.1%-23.6%, 5.2% -23.3%（Ce＋T1） and 10.8%-28.4%, 7.0%-27.8%（Ce＋T2）, lower than those of UV-B treatments. The decrease of growth indices appeared to be the result of changes of physiological processes. Two levels of UV-B radiation induced the decrease in chlorophyll content, net photosynthesis rate, transpiration rate, stomatal conductance and water use efficiency by 11.2%-25.9%（T1） and 20.9%- 56.9%（T2）, whereas increase in membrane permeability and activities of antioxidant enzymes including superoxide dismutase（SOD）, catalase （CAT） and peroxidase （POD） by 6.9%, 22.8%, 21.5%, 9.5%（T1） and 36.6%, 122.3%, 103.5%, 208.9%（T2）, respectively. The reduction of the photosynthetic parameters in Ce＋UV-B treatments was lessened to 3.2%-13.8%（Ce＋T1） and 4.9%-27.6%（Ce＋T2）, and the increase of membrane permeability and activities of antioxidant enzymes except POD in the same treatments were lessened to 2.4%, 8.4%, 6.6%（Ce＋T1） and 30.1%, 116.7%, 75.4%（Ce＋T2）. These results indicate that the regulative effect of Ce on photosynthesis and antioxidant enzymatic function is the ecophysiological basis of alleviating the suppression of UV-B radiation on growth of seedlings. Furthermore, the protective effect of Ce on seedlings exposed to TI level of UV-B radiation is superior to T2 level.     

基于TiO2载体的锰铈系低温SCR脱硝催化剂研究进展

开发低温、高活性、高抗硫抗水性能的选择性催化还原(SCR)脱硝催化剂已成为国内外的研究热点。综述了基于TiO2载体的锰铈系低温脱硝催化剂的脱硝性能,探讨了助剂掺杂改性、制备方法、反应条件等对催化剂脱硝性能的影响,总结了现有低温脱硝催化剂的技术难点,指出SCR催化剂的研究需要着重考虑以下几方面:深入研究催化剂的反应机理和中毒机理;研究催化剂的循环再生;探究拓宽催化剂温度窗口,使其适应不同的温度条件。     

Ozone facilitated degradation of caffeine using Ce-TiO2 catalyst

The ozone initiated oxidation of 1,3,7-trimethylxanthine (caffeine), commonly found in wastewaters as model compound is reported using cerium (Ce)/titanium dioxide (TiO₂) as catalyst. The effect of pH and loading of ceria on titania were investigated. Effect of reaction conditions on degradation of caffeine based on their pseudo first-order rate constants were compared. The combination of catalyst Ce-TiO₂ and ozone aeration significantly enhanced the degradation of caffeine compared to uncatalysed ozonation. The oxidation of caffeine ensued via the free radical mechanism, through enhanced ozone decomposition into OH radicals. Ce/TiO₂(0.5?wt%) showed good activity in degradation of caffeine at pH 6, in both natural stream and river water samples showing about 60% total organic carbon removal in 2?h ozonation period. Using liquid chromatography-mass spectroscopy, degradation products were analysed. A reaction intermediate and one final product were positively identified. Nano-catalysts with different loadings of Ce on TiO₂ synthesized by sol-gel route were characterized by scanning electron microscope, transmission electron microscopy, BET and powder X-ray diffraction spectrum techniques. The results showed that the material retained a highly ordered mesoporous structure and possessed large surface area.     

Modification of ferrite–manganese oxide sorbent by doping with cerium oxide

Fe–Mn oxide and Ce-doped Fe–Mn oxide sorbents were studied on the structural and desulfurization behavior in COS removal from syngas. The effects of cerium oxide on the Fe–Mn oxides have been investigated by XRD, BET, TPR, XPS and TEM methods. Analysis data show that the Ce-doped sorbent has larger specific surface area and better particles’ dispersion compared with non-modified Fe–Mn sorbent. The addition of Ce improves the reduction performance of Fe–Mn species. The desulfurization experiments show that the desulfurization activity of sorbent can be increased because of the promotion of the structural and redox properties by ceria doped. The Ce-doped sorbent can reduce COS from 15,000 ppmv to less than 0.1 ppmv at 325 °C and a space velocity of 1000 h⁻¹.     

V/Ce共掺杂TiO2光催化降解甲醛的实验研究

采用溶胶凝胶法制备了不掺杂、V 掺杂、Ce掺杂、V/Ce共掺杂纳米TiO₂光催化剂,并将其分别负载于瓷砖上,利用X射线衍射分析（XRD）和扫描电镜分析（SEM）技术对薄膜样品的结构和形貌进行了表征。通过对甲醛的降解实验评价光催化剂的光催化活性。实验结果表明,光催化剂的负载量、共掺杂离子的掺杂量、掺杂配比、煅烧温度影响纳米TiO₂的光催化活性。V/Ce共掺杂TiO₂光催化剂产生了协同效应,其光催化活性优于纯TiO₂和单掺杂TiO₂样品。     

Cu–Mn–Ce ternary mixed-oxide catalysts for catalytic combustion of toluene

Cu–Mn, Cu–Mn–Ce, and Cu–Ce mixed-oxide catalysts were prepared by a citric acid sol–gel method and then characterized by XRD, BET, H₂-TPR and XPS analyses. Their catalytic properties were investigated in the toluene combustion reaction. Results showed that the Cu–Mn–Ce ternary mixed-oxide catalyst with 1:2:4 mole ratios had the highest catalytic activity, and 99% toluene conversion was achieved at temperatures below 220°C. In the Cu–Mn–Ce catalyst, a portion of Cu and Mn species entered into the CeO₂ fluorite lattice, which led to the formation of a ceria-based solid solution. Excess Cu and Mn oxides existed on the surface of the ceria-based solid solution. The coexistence of Cu–Mn mixed oxides and the ceria-based solid solution resulted in a better synergetic interaction than the Cu–Mn and Cu–Ce catalysts, which promoted catalyst reducibility, increased oxygen mobility, and enhanced the formation of abundant active oxygen species.